Disease: Hypertensive disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.330 GeneticVariation group BEFREE In humans, ERAP1 rs30187, a loss-of-function gene variant that reduces ANGII degradation in vitro, is associated with hypertension. 31672933 2019
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.330 AlteredExpression group BEFREE The reduced enzymatic activity of A-LAP may cause high blood pressure and the observed association between the polymorphism and hypertension. 16513116 2006
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.330 Biomarker group CTD_human Adipocyte-derived leucine aminopeptidase genotype and response to antihypertensive therapy. 13678427 2003
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.330 GeneticVariation group LHGDN We considered the hypothesis that genomic variants of the ALAP gene are associated with hypertension or individual variations in blood pressure. 11857741 2002
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.330 GeneticVariation group BEFREE We considered the hypothesis that genomic variants of the ALAP gene are associated with hypertension or individual variations in blood pressure. 11857741 2002